The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
123373282 12337328 2 F 20160725 20160505 20160802 EXP CA-PFIZER INC-2016241844 PFIZER 45.00 YR F Y 76.00000 KG 20160802 CN CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
123373282 12337328 1 SS ENBREL ETANERCEPT 1 Unknown UNK UNK, WEEKLY U 0 /wk
123373282 12337328 2 PS IBUPROFEN. IBUPROFEN 1 Unknown UNK U 18989
123373282 12337328 3 SS HUMIRA ADALIMUMAB 1 Unknown UNK U 0
123373282 12337328 4 SS ORENCIA ABATACEPT 1 Unknown UNK U 0
123373282 12337328 5 SS REMICADE INFLIXIMAB 1 Unknown UNK U 0
123373282 12337328 6 SS RITUXAN RITUXIMAB 1 Unknown UNK U 0
123373282 12337328 7 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Oral 200 MG, 2X/DAY 0 200 MG BID
123373282 12337328 8 C METHOTREXATE. METHOTREXATE 1 Oral 10 MG, WEEKLY 0 10 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123373282 12337328 1 Rheumatoid arthritis
123373282 12337328 2 Rheumatoid arthritis
123373282 12337328 3 Rheumatoid arthritis
123373282 12337328 4 Rheumatoid arthritis
123373282 12337328 5 Rheumatoid arthritis
123373282 12337328 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
123373282 12337328 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123373282 12337328 Drug ineffective
123373282 12337328 Injection site reaction
123373282 12337328 Renal impairment
123373282 12337328 Rheumatoid arthritis
123373282 12337328 Throat tightness

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found